Clinical Research Coordinator II

Clinical Research Coordinator II


Job ID: 9784771

Miami, FL, US

Scientific

Bachelors Degree

Full Time, Temporary

26.17-$29.08/hr.

Entry Level

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Miami, FL, US

26.17-$29.08/hr.

Entry Level

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Job details

Clinical Research Coordinator II
Day shift 
On Site
6 month assignment
Pay Rate: $26.17-$29.08/hr.

What’s a typical day as Clinical Research Coordinator? You’ll be:

  • Conducting clinical studies in accordance with FDA, GCP, and ICH regulations and guidelines.

  • Providing medical care to patients, always prioritizing patient safety.

  • Scheduling subject visits, maximizing scheduling capacity, and ensuring protocol compliance.

  • Performing all defined study activities, such as informed consent, screening, and protocol procedures (vital signs, pregnancy tests, height, weight, ECGs, etc.).

  • Recording patient information and test results per protocol on required forms.

  • Completing IP accountability logs as required and reporting suspected non-compliance.

  • Ensuring IRB approval is obtained before study initiation and maintaining IRB requirements throughout the study.

  • Building positive patient relationships to promote retention and attending meetings for protocol training.

  • Managing patient bookings, follow-up calls, and accurate data entry into sponsor systems.

  • Maintaining source documents and updating patient files to ensure accurate and updated records.

  • Adhering to company policies and maintaining a neat facility environment.

This job might be an outstanding fit if you:

  • Hold a bachelor’s degree or equivalent formal academic/vocational qualification in the clinical or medical field.

  • Possess a valid nursing license (RN, LVN, LPN) and are registered with the local healthcare authority.

  • Have 2+ years of relevant clinical research or healthcare experience.

  • Demonstrate a solid understanding of the clinical research process (GCP, SOPs, informed consent, safety monitoring, etc.).

  • Can work independently, analyze and prioritize complex information, and solve problems with attention to detail.

  • Exhibit good decision-making, negotiation, and influencing skills.

  • Communicate effectively (English fluency is an advantage) and possess strong interpersonal and organizational skills.

  • Are proficient in basic computer applications and enjoy working in a team environment.

What happens next

Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.

Helping you discover what’s next in your career is what we’re all about, so let’s get to work. Apply to be Clinical Research Coordinator today!

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